Pulsenet Timeline

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Pulsenet Timeline PulseNet is a national laboratory network that connects foodborne illness cases to detect outbreaks. PulseNet uses DNA fingerprinting, or patterns of bacteria making people sick, to detect thousands of local and multistate outbreaks. Since the network began in 1996, PulseNet has improved our food safety systems through identifying outbreaks early. This allows investigators to find the source, alert the public sooner, and identify gaps in our food safety systems that would not otherwise be recognized. E. coli O157:H7 is first recognized as a significant human pathogen. 1984 Pulsed-field gel electrophoresis (PFGE), the current gold standard for DNA fingerprinting, is developed by Schwartz and Cantor. 1993 E. coli O157:H7 causes a major outbreak in the Western US states. 1994 CDC and several state health laboratories demonstrate the utility of 1995 PFGE for detecting and investigating » The concept of PulseNet takes outbreaks of foodborne disease. shape in discussions between CDC, the Association of Public Health Laboratories (APHL), state public 1996 health laboratories and federal » CDC launches PulseNet with partners. the APHL, federal partners, and the original area public health » CDC provides $150,000 to PulseNet laboratories in Massachusetts, to conduct an initial project Minnesota, Texas, and Washington. demonstrating its effectiveness. » The first PulseNet training for standardized PFGE and analysis 1997 of patterns is organized at CDC. » PulseNet detects an outbreak of The area laboratories and the U.S. E. coli O157:H7 in Colorado linked to Department of Agriculture Food frozen ground beef from a Nebraska Safety and Inspection Service processing plant. Twenty-five million (USDA) laboratories attend. pounds of potentially contaminated ground beef are recalled. » CDC establishes the Epidemiology Laboratory Capacity (ELC) building program. This program funds public health laboratories to join PulseNet. 1998 PulseNet is honored by the Vice » The U.S. Food and Drug President of the United States at a Administration’s (FDA) Center for Food White House ceremony. Safety and Applied Nutrition (CFSAN) laboratory joins PulseNet. 1999 » The National Food Safety Initiative is PulseNet wins the Innovations in established, detailing how $43.2 million American Government Award, is to be used to strengthen food safety recognizing excellence and creativity in the US. PulseNet becomes one of in the public sector. the first CDC-established networks that this initiative supports. 2000 PFGE analysis software is provided 2001 by APHL to all existing PulseNet PulseNet becomes a nationwide laboratories allowing the creation of system: all 50 state public health organized databases. laboratories are trained and certified in PFGE. 2002 PulseNet wins the prestigious Innovations in American Government Award for the second time. 2004 2005 CDC pilots the Listeria Initiative in » Manufacturers introduce the 10 states to aid in the investigation first commercially available next- of listeriosis clusters detected by generation DNA sequencing system. PulseNet, decreasing the time from Next-generation sequencing detection to stopping the outbreak. technologies will shape the future of PulseNet and accelerate outbreak 2006 detection. PulseNet links contaminated » PulseNet integrates multiple bagged spinach to a large multistate locus variable number tandem outbreak of E. coli O157:H7, prompting repeat analysis (MLVA) as a a nationwide recall. The outbreak genotyping tool for E. coli O157:H7 sickens 225 people in 27 states and and Salmonella enterica serotype causes 39 cases of kidney failure and Typhimurium. 5 deaths. 2009 PulseNet links peanut butter and peanut products to a multistate outbreak of Salmonella Typhimurium. The infection sickens over 700 people in 46 states and causes 9 deaths. More than 3,000 2010 types of peanut-containing products are Whole genome sequencing is used for recalled. the first time in an ongoing outbreak investigation. PulseNet performs real- time sequencing on three samples from a Vibrio cholerae outbreak that killed thousands in Haiti. 2011 » PulseNet begins analyzing data using bioinformatics, which combines biology, 2013 computers, and information technology PulseNet scientists begin using whole in a single discipline to answer pressing genome sequencing methods, along public health questions. » 250 historic isolates of Shiga-toxin with enhanced disease investigation, to producing E. coli (STEC) are sequenced study foodborne illnesses caused by to prove the utility of whole genome Listeria. sequencing for surveillance of foodborne pathogens. » Congress passes the FDA Food Safety Modernization Act (FSMA) and directs CDC to expand national foodborne disease surveillance systems. 2014 » CDC launches the “Transforming Public Health Microbiology – PulseNet and 2015 Beyond” project under the Advanced » The Listeria study receives the CDC Molecular Detection (AMD) initiative, Director’s Award for Innovation which aims to consolidate most » CDC routinely uses whole genome foodborne pathogen identification sequencing for investigating and characterization activities into a foodborne illnesses caused by Listeria, single, fast, and efficient whole genome Campylobacter, Shiga toxin-producing sequencing process. E. coli, and Salmonella. » The Listeria whole genome sequencing study, that began in 2013, receives the 2016 Department of Health and Human » Whole genome sequencing is used Services (HHS) Innovates Secretary’s for routine surveillance of Listeria, Pick award for implementing an Campylobacter, and Shiga toxin- innovative strategy to address an producing E. coli (STEC). emerging public health challenge. » PulseNet can analyze Salmonella whole genome sequencing data to investigate outbreaks. » The American Journal of Preventive 2017 Medicine publishes an economic evaluation that suggest that PulseNet » Whole genome sequencing will be used prevents at least 270,000 illnesses for routine surveillance of Salmonella from Salmonella, E. coli, and Listeria and in states that have the capacity to saves $500,000 US dollars every year. conduct sequencing. » PulseNet will be able to analyze Vibrio and Shigella whole genome sequencing data. 2018 2020 and Beyond 2020 » PulseNet will be able to analyze Yersinia and Cronobacter whole genome PulseNet will use highly sophisticated sequencing data. approaches designed to identify and » All 50 state public health laboratories subtype foodborne pathogens directly will be using whole genome sequencing from complex clinical samples, without for routine surveillance. bacterial cultures. The favored approach, » Whole genome sequencing will become known as metagenomics, has the the new PulseNet gold standard for potential to allow extraction of subtyping pathogens that cause pathogen-specific DNA sequence foodborne illness. information directly from complex samples such as stool. Before PulseNet 5 years 10 years 20 years The Future of PulseNet U.S. Department of Health and Human Services Centers for Disease Control and Prevention CS263215B.
Recommended publications
  • In Silico Characteristics for Re-Emerging Possibility of Vibrio Cholerae Genotypes in Iran
    ORIGINAL ARTICLE In silico characteristics for re-emerging possibility of Vibrio cholerae genotypes in Iran M. Hajia1 and Amir Sohrabi2 1) Department of Molecular Biology, Research Center of Health Reference Laboratory, Ministry of Health and Medical Education, Tehran, Iran and 2) Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden Abstract Epidemic cholera has been registered several times within recent years in Iran. The dominant genotype was Ogawa until 2011, but this gradually changed to Inaba. However, in 2015, the re-appearance of a previous Ogawa genotype was detected by the Iranian CDC. This raised worries because no evidence was found for its origin abroad. The aim of the present study was to identify clearly the source of this outbreak. Pulsed field gel electrophoresis (PFGE) was used to compare the recently detected Vibrio cholerae strains with those isolated from 2011 to 2015. We selected one strain per PFGE pattern, and compared the distinct patterns. BIONUMERICS software was applied, which enables interpretation of phenotypic and genotypic differences. In total, we studied 33 V. cholerae Ogawa strains. Analysis showed that strains could be discriminated on the basis of annual clusters but with a similarity of more than 80%. The highest homology was observed among those isolated each year from 2011 to 2014. In contrast, strains isolated in 2015 also exhibited close correlation with each other but were located in distinct clusters. The analysis also proved genetic variations among some strains. All 2015 strains showed differences with regard to previous genotypes despite some similarities. The new genotypes were probably imported into Iran from neighbouring countries such as Iraq by travellers or contaminated food sources since 2015.
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  • Pulsenet: Depicting Red-Colored Salmonella Bacteria Invading a Mustard- Colored, Ruffled Immune Cell
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  • Pulsenet International
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  • Pulsenet: on the Front Lines of Foodborne Disease Surveillance
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  • Blank CDC Letterhead for Outgoing Correspondence
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  • Pulsed-Field Gel Electrophoresis (PFGE) a Review of the “Gold
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  • Molecular Surveillance of Shiga Toxigenic Escherichia Coli O157 by Pulsenet USA
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  • Pulsenet: 20 Years of Making Food Safer to Eat
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  • Chapter I: History and Trends
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  • Standard Operating Procedure for Pulsenet Pfge of Escherichia Coli O157:H7, Escherichia Coli Non-O157 (Stec), Salmonella Serotyp
    Standard Operating Procedure for PulseNet PFGE of Escherichia coli O157:H7, Escherichia coli non-O157 (STEC), Salmonella serotypes, Shigella sonnei and Shigella flexneri Purpose To describe the One-Day (24-26 hour) Standardized Laboratory Protocol for Molecular Subtyping of E. coli O157:H7, E. coli Non-O157 (STEC), Salmonella, Shigella sonnei and Shigella flexneri by Pulsed-field Gel Electrophoresis (PFGE). Scope To provide the PulseNet participants with a standardized procedure for performing PFGE of E. coli O157:H7, E. coli Non- O157 (STEC), Salmonella, Shigella sonnei and Shigella flexneri, thus ensuring inter-laboratory comparability of the generated results. Definitions and Terms 1. PFGE: Pulsed-field Gel Electrophoresis 2. DNA: Deoxyribonucleic acid 3. CDC: Centers for Disease Control and Prevention 4. CLRW: Clinical Laboratory Reagent Water 5. TE: Tris-EDTA 6. EDTA: Ethylenediaminetetraacetic Acid 7. TBE: Tris borate-EDTA 8. HIA: Heart Infusion Agar Biosafety Warning Escherichia coli O157:H7, Salmonella serotypes, Shigella sonnei, and Shigella flexneri are human pathogens and can cause serious disease. It has been reported that less than 100 cells of E. coli O157:H7 may cause infection. Shigella species also have a low infectious dose and are demonstrated hazards to laboratory personnel. Always use Biosafety Level 2 practices (at a minimum) and extreme caution when transferring and handling strains of these genera. Work in a biological safety cabinet when handling large amounts of cells. Disinfect or dispose of all plasticware and glassware that come in contact with the cultures in a safe manner. Please read all instructions carefully before starting protocol. It is recommended to plate cultures, prepare cell suspensions, and cast plugs in a Class II Biosafety Cabinet (BSC), if available.
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